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Keywords : MD, medical doctor, consultant, medical monitor, early clinical development, oncology, cancer, solid tumors, small molecules, targeted therapy, clinical trial, study, protocol, asset, pharma, biotech, biopharma, MD, phase I, first-in-human, FIH, IND, phase II, FDA.
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Our client is a clinical-stage biopharma company developing precision oncology medicines using its proprietary proteomics platform to develop drug-specific companion diagnostics. Our client is a clinical-stage biopharma company developing precision oncology medicines using its proprietary proteomics platform to develop drug-specific companion diagnostics.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Alnylam is extremely proud to have been recognized as the #1 Large Employer by Boston Globe Top Places to Work in 2022, one of Science Magazine's Top Biopharma Employers, one of America's Most Responsible Companies for 2023 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK - among others.
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Join FDB and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. Join FDB and help manufacture the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe.
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Job Title: Principal - Biopharma Strategy Consulting. A strong understanding of dynamics and issues in the biopharma industry (required) I am working directly with the founders of a rapidly growing privately owned consulting firm where making a difference is woven into their DNA, pushing at length their patient centric philosophy and head up by some of the industries most prestigious leaders.
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Bachelors degree and 2 years of related medical/biopharma development or Operations experience; OR. We are interested in seeing candidates with Masters or Bachelors in Engineering and at least 2 years of experience related medical/biopharma development or Operations experience.
$37 - $40 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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The Materials Control Associate III is accountable for GMP (Good Manufacturing Practices) materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility. The Materials Control Associate III is accountable for GMP (Good Manufacturing Practices) materials control/warehousing operations for a Phase II/III GMP biopharma manufacturing facility.
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Must have experience working in the Life Sciences (Medical Device/Biopharma) VTI Life Sciences strives to maintain and inspire professional excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries.
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That's why we were named the No. 1 company to work for in the biopharma industry in Science's Top Employers Survey for two years in a row. If you share our vision and want to work with the most dedicated people in the biopharma industry, come to Insmed to accelerate your career.
$146Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Catalent Biologics in Bloomington, Indiana is a state-of-the art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services.
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Bridge to thousands of biopharma companies and their patients. Attend Tier I Daily Directional Setting (DDS) meeting. Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.
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Our teams help biopharma, medical device and emerging diagnostic companies get their therapies to the people who need them. In partnership with our client, we are currently looking for Oncology Diagnostic Sales Specialists to promote diagnostic pathology tests across the full catalogue of client offerings in various therapeutic areas specific to Hematology, Oncology and specific Infectious Disease.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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All resumes submitted by search firms or employment agencies to any employee at KBI Biopharma via-email, telephone, social media or other means will be deemed to be the sole property of KBI Biopharma, unless the firm submitting the resume has.
$65,000 - $85,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Extensive knowledge of CRO clinical trial execution and operations, preferably through direct experience working for a CRO, biopharma, or as a service provider to a CRO. Labcorp Drug Development Data & Digital Solutions (D&DS) is currently in search of Product Manager to drive Discovery and Solution development for a family of products.
$104,200 - $143,300 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago
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